Synthesis of proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway

Org Lett. 2003 Sep 4;5(18):3233-6. doi: 10.1021/ol035101r.

Abstract

[structure: see text] A chemoenzymatic synthesis was described to prepare proposed oxidation-cyclization-methylation intermediates of the coumarin antibiotic biosynthetic pathway. The successful synthesis of these fragile molecules relies heavily on mild enzymatic deprotection and efficient enzymatic kinetic resolution to minimize epimerization, decomposition, multiple orthogonal protections, and retro aldol reactions often encountered in their chemical synthesis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Catalysis
  • Coumarins / chemical synthesis*
  • Cyclization
  • Endopeptidases / chemistry
  • Esterases / chemistry
  • Keto Acids / chemistry
  • Kinetics
  • Lipase / chemistry
  • Methylation
  • Molecular Structure
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Anti-Bacterial Agents
  • Coumarins
  • Keto Acids
  • Esterases
  • Lipase
  • Endopeptidases